Canonical Allele Identifier: CA520118784
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21645130C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19483244C>A , CM000686.2:g.19483244C>A GRCh38
NC_000024.9:g.21645130C>A , CM000686.1:g.21645130C>A GRCh37
NC_000024.8:g.20104518C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-2950G>T
ENST00000400605.5:n.106-2950G>T
ENST00000441139.5:n.123-2950G>T
ENST00000513194.1:n.1641G>T
NR_002923.2:n.123-2950G>T
NR_033732.1:n.123-2950G>T
Search 100 bp 5'
Search 100 bp 3'